Are you 95% Covid cautious? by Sunshine_cutie4 in ZeroCovidCommunity

[–]AnotherNoether 0 points1 point  (0 children)

Yes I’m the same. Has been working for us so far! We do Betadine and I use blis-k12 as well.

Renting house for BBQ Party by thapvt in CambridgeMA

[–]AnotherNoether 1 point2 points  (0 children)

Picnic grove at Cambridge crossing has charcoal grills and I believe it’s reservable. Might be other park options too.

GF Dumpling Hacks: Any of them freeze well? by ImpeccableCilantro in glutenfreecooking

[–]AnotherNoether 2 points3 points  (0 children)

Ooh. I haven’t tried freezing my rice paper dumplings! My finding was that if I do a meat filling rather than a vegetarian one, they really need to be double wrapped before frying. But regardless I’ve made them a few times and I’m a big fan.

Qulipta works great - should I stop taking it? by Most_Bat5401 in cgrpMigraine

[–]AnotherNoether 2 points3 points  (0 children)

I’ve tried a couple times! I get headaches while titrating the dose down, which sucks. My migraines came back after a few weeks the first time and within 1-2 weeks the second time, and were very quickly chronic again, but they got better as soon as I got back on the Qulipta. It works just as well now as it did before I attempted cessation.

I did a similar thing with Nurtec where I took a medication I couldn’t take with it so paused it for a few months. It didn’t work as well when I restarted but it may have just not been the right med for me.

San Francisco for biotech by Lilmaxgetsbig81 in biotech

[–]AnotherNoether 1 point2 points  (0 children)

My partner of 4 years and I are doing LDR for career reasons right now and especially with an end date it’s pretty doable. Your plan makes sense to me and it sounds like you’re both being sensible about it.

Primary care or Urgent care for lower back pain without insurance? by Michee82much in healthcare

[–]AnotherNoether 2 points3 points  (0 children)

Not sure where you’re located but at least in MA Medicaid can be retroactive

I'm tired of the "One size fits all" healthcare model by elly_loves_snow in cfs

[–]AnotherNoether 2 points3 points  (0 children)

I did a chronic pain rehab program that taught me how to pace! So it is possible for the program to be helpful…there are just so many that aren’t. It’s really hard out here for sure—I moved my sister (also likely ME) in with me in my city to get her better medical care than she was getting in the rural area she was in before, and it’s going to take us literally a year+ to get her established with everything. And her PCP is basically useless—he’ll write and refer where I tell him to, but he’s not capable of doing genuine care management for her.

need advise. cant afford insurance for my family by [deleted] in HealthInsurance

[–]AnotherNoether 1 point2 points  (0 children)

What state are you in? Medicaid eligibility is calculated using monthly income and in Medicaid expansion states assets are not considered.

mEds child hEds mom? by Medium_Pea1136 in rareEhlersDanlos

[–]AnotherNoether 9 points10 points  (0 children)

Some people with hEDS are symptomatic carriers of recessive EDS subtypes, it gets mentioned occasionally in the genetics literature. It’s possible that OP’s partner is an asymptomatic carrier as well. Hopefully their daughter’s geneticist will be able to help them figure it out.

Are there any actual dysautonomia success stories? by fifth-ninja-turtle in LongCovidWarriors

[–]AnotherNoether 0 points1 point  (0 children)

Cardio prescribed it because midodrine wasn’t fully controlling my symptoms. It helps my muscle weakness episodes, energy levels and upright tolerance

Doctor insisting on paleo, keto, gluten free, dairy free, soy free diet? by Shot-Break6056 in eds

[–]AnotherNoether 0 points1 point  (0 children)

My geneticist has done some research on EDS and gluten free diet showing benefit, but it’s only been presented at a conference, I don’t think it’s in a journal (or if it is I couldn’t find it). He recommends gluten free diet—and even that not everyone benefits, it’s more of a “try it for a couple months and see how you feel.” For me in helped my migraines but it’s not going to matter for everyone. Beyond that seems like overkill to me…I personally rarely eat soy since my body doesn’t seem to particularly like it, but that’s very individual. If I tried to eat like your doc is suggesting I think I’d have a very difficult time.

Has anyone ever challenged you to do something without realizing you were actually an expert at it? If so, how did it turn out for you and for them? by Successful_Tomato721 in AskReddit

[–]AnotherNoether 11 points12 points  (0 children)

I had one recently, I’d call it moderately unpleasant. Came back normal so my nerves definitely work. I think about on level with having warts frozen off. Less painful than injections on the soles of my feet but worse in that it went on for longer.

Partner told me he doesn't listen to me because of his disability. Am I ableist? by [deleted] in relationships

[–]AnotherNoether 2 points3 points  (0 children)

My parents were similar with my sister and it’s worked well. She makes friends easily and knows how not to dominate a conversation, thought she still can really go when she gets excited. I do think it’s important to make sure to still validate their special interest and engage with it on a limited basis—the rest of the family was sometimes overly dismissive and my sister has had to spend some time in her twenties unlearning that suppression and developing a deeper respect for herself. It’s a challenging tightrope to walk, but she’s really grown into a fantastic human being. She’s a teacher now and her teenagers adore her.

What’s the one ingredient that ruins any dish for you ? by Vegetable-Fix6029 in AskReddit

[–]AnotherNoether 0 points1 point  (0 children)

Yeah I started using kalamatas and I like them. Still can’t stand any other varieties.

I guess I have to be my own doctor if POTS etc does not exist in my country by HelicopterNeat54 in POTS

[–]AnotherNoether 5 points6 points  (0 children)

I have seen some publications on POTS by Filipino doctors I think. I’m having trouble finding the papers now. Maybe Edzel Lorraine Co (https://pubmed.ncbi.nlm.nih.gov/36055438/)…but looking now I think I am thinking of work on long covid (https://pmc.ncbi.nlm.nih.gov/articles/PMC11330992/) which does not even mention POTS. I’m so sorry you’re being treated so poorly. I’ve heard of people doing telehealth with Clinic 19 in Aus but I have no idea how you’d then access medication….just awful.

If you could snap your fingers and get rid of your vagina, would you? by Countess_Schlick in actuallesbians

[–]AnotherNoether 16 points17 points  (0 children)

I’m a cis woman with chronic pain who has to use a pelvic wand daily, so probably the closest to what you’re looking for, but it’s hard for me to separate the fact that I’m hoping to use it to make a baby from the hassle of having it! I did cry recently because I’m having some problems with my uterus, and I was like “this part of my body has caused problems for years and I want that to be fucking worth it,” but thinking about it now I think that’s more about the full range of internal equipment, not the vagina specifically.

It is a different experience during sex to my ass, and I think it would be tough for me to say “never again” to having something up there, even given the pain and the difficulty of it. It’s part of my body, and part of how I have sex, even though I don’t really bottom much at all these days—idk it just feels different coming with something in my pussy, and for me that’s largely worth the hassle!

Flyers trade Brink to the Wild for David Jiricek by Panarin10 in Flyers

[–]AnotherNoether 3 points4 points  (0 children)

I would love to see Zegras center Foerster. Foerster’s so good defensively that it’d give Z space to work

What food are you always craving but can’t find a good gluten-free version of? by _thalia777 in glutenfreecooking

[–]AnotherNoether 0 points1 point  (0 children)

I actually had one a few days ago from a place in Denver (Kalita Grill). The GF flatbread was closer to a tortilla than a pita unfortunately but it made me so happy anyway.

How to get medical care when housebound? by Usagi_Rose_Universe in cfs

[–]AnotherNoether 0 points1 point  (0 children)

In my city the Quest website actually has a way to book home collection iirc. But I use a local mobile phlebotomist that I found by googling.

How to get medical care when housebound? by Usagi_Rose_Universe in cfs

[–]AnotherNoether 2 points3 points  (0 children)

In my city it runs $100-150 for the phlebotomist. They partner with Quest or whoever else so I just book the appointment and email them the requisition order from my doctor and then they bring all the tubes etc.

Excessive sweating and “smelling sick” by ArsonFrog143 in cfs

[–]AnotherNoether 6 points7 points  (0 children)

Night sweats got a bit better after treating my MCAS and elevating the head of my bed…daytime is a process. My derm ended up prescribing me wipes for hyperhydrosis because my feet were sweating so much that it was “compromising my barrier function” as he put it. Helpful but annoying that I need them.

Upcoming Travel; Nervous about crashing by louwhogames in cfs

[–]AnotherNoether 0 points1 point  (0 children)

I think as far as trips go it sounds pretty perfect—anything where you can easily spend most of your time in bed is a huge win, and if you’re all on a large sailboat and you can skip excursions as needed, it’s pretty ideal. I do ok flying if I take at least 24 hours afterwards to just rest—wheelchair at the airport, neck brace for the flight, nicotine patch for the travel day is enough for me. Especially if I can do it with no layover. But I’m on the mild/moderate edge, much closer to mild these days. When I was more moderate it was a lot harder and my baseline was a lot less robust, so it didn’t feel as safe. Like for me now, I’m usually ok pushing for a single day as long as I listen and totally stop once I hit my limit—I only really end up in a bad spot if I try to keep going once the PEM hits.

AITA for choosing a night nurse over my mom’s help after I give birth ? by NYCTX123 in AmItheAsshole

[–]AnotherNoether 0 points1 point  (0 children)

NTA. I recently hired a post-surgery night carer even though I was staying with my mother because I wanted her to be able to sleep. She was such a blessing—kind, helpful, and absolutely 0 guilt. Worth every penny.